The test report for the registration or filing of cosmetics must be issued by cosmetic registration and filing inspection institutions. The test report must conform with the requirements of the Technical Standards for Cosmetics, the Working Rules for Cosmetic Registration and Filing as well as other regulations.

CIRS is delighted to announce that we will be exhibiting at the PCHi in Hangzhou, China between 18-20 March, 2026.

On February 2, 2026, the Taiwan Food and Drug Administration (TFDA), under the Ministry of Health and Welfare, announced a revision to the annex of the Documentation Required for Case-by-Case Review of Applications for the Use of Human Cell-Derived Exosomes in Cosmetics. The revised annex takes effect immediately upon the date of announcement.

On November 24, 2025, the Taiwan Food and Drug Administration (TFDA) under the Ministry of Health and Welfare officially issued the testing method for Sudan dyes in cosmetics (Method No. RA03D015.001), which came into effect upon the date of publication.

This article compiles and summarizes the latest developments in cosmetics regulations in China and globally as of October 2025, covering industry news, newly issued regulations, relevant policy adjustments, and regulatory requirements. It aims to assist enterprises in ensuring compliance and keeping up with global cosmetics regulatory trends.

In our last article, Is Your Scalp Healthy? – Scalp Health Evaluation Methods (Part I), we have introduced the evaluation methods for dandruff, sebum levels, and itchiness. In this article, we will continue with the evaluation methods for erythema/papules/pustules and the overall hair status.

On June 6, 2025, CIRS Group officially launched the Global Cosmetic Ingredient Regulatory Database--Global CosIng. This database integrates regulatory information on cosmetic ingredients from major markets, including China (Taiwan included), the European Union, the United States, Canada, ASEAN countries, South Korea, and Japan. It is designed to provide enterprises with a one-stop, authoritative, and user-friendly platform for ingredient compliance inquiries, supporting cosmetic companies in global regulatory compliance and product development.

In-vitro Evaluation

This article compiles and summarizes the latest developments in cosmetics regulations in China and globally as of September 2025, covering industry news, newly issued regulations, relevant policy adjustments, and regulatory requirements. It aims to assist enterprises in ensuring compliance and keeping up with global cosmetics regulatory trends.

Since the concept of New Approach Methodologies (NAMs) was introduced, various methods including in vitro approaches, Threshold of Toxicological Concern (TTC), and computational models have gained favor among toxicological assessment experts. With the increasing capabilities of computational models, key toxicological endpoints such as acute toxicity, skin/eye irritation, sensitization, chronic toxicity, genotoxicity, carcinogenicity, reproductive and developmental toxicity, and toxicokinetics can now be predicted using QSAR models.